Structure and function of the feed-forward loop network motif.

@article{citeulike:159797, abstract = {Engineered systems are often built of recurring circuit modules that carry out key functions. Transcription networks that regulate the responses of living cells were recently found to obey similar principles: they contain several biochemical wiring patterns, termed network motifs, which recur throughout the network. One of these motifs is the feed-forward loop (FFL). The FFL, a three-gene pattern, is composed of two input transcription factors, one of which regulates the other, both jointly regulating a target gene. The FFL has eight possible structural types, because each of the three interactions in the FFL can be activating or repressing. Here, we theoretically analyze the functions of these eight structural types. We find that four of the FFL types, termed incoherent FFLs, act as sign-sensitive accelerators: they speed up the response time of the target gene expression following stimulus steps in one direction (e.g., off to on) but not in the other direction (on to off). The other four types, coherent FFLs, act as sign-sensitive delays. We find that some FFL types appear in transcription network databases much more frequently than others. In some cases, the rare FFL types have reduced functionality (responding to only one of their two input stimuli), which may partially explain why they are selected against. Additional features, such as pulse generation and cooperativity, are discussed. This study defines the function of one of the most significant recurring circuit elements in transcription networks.}, address = {Departments of Molecular Cell Biology and Physics of Complex Systems, Weizmann Institute of Science, Rehovot 76100, Israel.}, author = {Mangan, S. and Alon, U. }, citeulike-article-id = {159797}, doi = {10.1073/pnas.2133841100}, issn = {0027-8424}, journal = {Proc Natl Acad Sci U S A}, month = {October}, number = {21}, pages = {11980--11985}, posted-at = {2007-10-10 00:48:43}, priority = {2}, title = {Structure and function of the feed-forward loop network motif.}, url = {http://dx.doi.org/10.1073/pnas.2133841100}, volume = {100}, year = {2003} }

TY - JOUR ID - citeulike:159797 L3 - citeulike-article-id:159797 TI - Structure and function of the feed-forward loop network motif. JF - Proc Natl Acad Sci U S A VL - 100 IS - 21 SP - 11980 EP - 11985 AD - Departments of Molecular Cell Biology and Physics of Complex Systems, Weizmann Institute of Science, Rehovot 76100, Israel. SN - 0027-8424 N2 - Engineered systems are often built of recurring circuit modules that carry out key functions. Transcription networks that regulate the responses of living cells were recently found to obey similar principles: they contain several biochemical wiring patterns, termed network motifs, which recur throughout the network. One of these motifs is the feed-forward loop (FFL). The FFL, a three-gene pattern, is composed of two input transcription factors, one of which regulates the other, both jointly regulating a target gene. The FFL has eight possible structural types, because each of the three interactions in the FFL can be activating or repressing. Here, we theoretically analyze the functions of these eight structural types. We find that four of the FFL types, termed incoherent FFLs, act as sign-sensitive accelerators: they speed up the response time of the target gene expression following stimulus steps in one direction (e.g., off to on) but not in the other direction (on to off). The other four types, coherent FFLs, act as sign-sensitive delays. We find that some FFL types appear in transcription network databases much more frequently than others. In some cases, the rare FFL types have reduced functionality (responding to only one of their two input stimuli), which may partially explain why they are selected against. Additional features, such as pulse generation and cooperativity, are discussed. This study defines the function of one of the most significant recurring circuit elements in transcription networks. AU - Mangan, S AU - Alon, U PY - 2003/10/14/ UR - http://dx.doi.org/10.1073/pnas.2133841100 ER -